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Roberta Tammaro

Showing results (1-10 of 16) with videos related to

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American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|February 3, 2022
OFD1: One gene, several disordersNunziana Pezzella, Guglielmo Bove, Roberta Tammaro, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 8, 2006
Apoptosis in retinal degeneration involves cross-talk between apoptosis-inducing factor (AIF) and caspase-12 and is blocked by calpain inhibitorsDaniela Sanges, Antonella Comitato, Roberta Tammaro, et al.
Scientific Reports|June 7, 2016
Synthetic long non-coding RNAs [SINEUPs] rescue defective gene expression in vivoAlessia Indrieri, Claudia Grimaldi, Silvia Zucchelli, et al.
Plos One|January 10, 2013
Ofd1 controls dorso-ventral patterning and axoneme elongation during embryonic brain developmentAnna D'Angelo, Amalia De Angelis, Bice Avallone, et al.
Human Mutation|March 22, 2006
Aberrant splicing in the ocular albinism type 1 gene (OA1/GPR143) is corrected in vitro by morpholino antisense oligonucleotidesFrancesco Vetrini, Roberta Tammaro, Sergio Bondanza, et al.
Human Molecular Genetics|November 3, 2018
The deubiquitinating enzyme Usp14 controls ciliogenesis and Hedgehog signalingFilomena Massa, Roberta Tammaro, Miguel A Prado, et al.
Tissue & Cell|June 1, 2020
The centrosomal/basal body protein OFD1 is required for microtubule organization and cell cycle progressionMariaevelina Alfieri, Daniela Iaconis, Roberta Tammaro, et al.
Developmental Biology|October 6, 2010
Ofd1 is required in limb bud patterning and endochondral bone developmentSabrina Bimonte, Amalia De Angelis, Luca Quagliata, et al.
American Journal of Human Genetics|November 6, 2012
Mutations in COX7B cause microphthalmia with linear skin lesions, an unconventional mitochondrial diseaseAlessia Indrieri, Vanessa Alexandra van Rahden, Valeria Tiranti, et al.
European Journal of Human Genetics : EJHG|April 21, 2026
Revisiting LSDMCA: male lethality escape and genotype-phenotype correlationsAlfonso Manuel D'Alessio, Alessia Indrieri, Giuseppina Vitiello, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|February 3, 2022
OFD1: One gene, several disordersNunziana Pezzella, Guglielmo Bove, Roberta Tammaro, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 8, 2006
Apoptosis in retinal degeneration involves cross-talk between apoptosis-inducing factor (AIF) and caspase-12 and is blocked by calpain inhibitorsDaniela Sanges, Antonella Comitato, Roberta Tammaro, et al.
Scientific Reports|June 7, 2016
Synthetic long non-coding RNAs [SINEUPs] rescue defective gene expression in vivoAlessia Indrieri, Claudia Grimaldi, Silvia Zucchelli, et al.
Plos One|January 10, 2013
Ofd1 controls dorso-ventral patterning and axoneme elongation during embryonic brain developmentAnna D'Angelo, Amalia De Angelis, Bice Avallone, et al.
Human Mutation|March 22, 2006
Aberrant splicing in the ocular albinism type 1 gene (OA1/GPR143) is corrected in vitro by morpholino antisense oligonucleotidesFrancesco Vetrini, Roberta Tammaro, Sergio Bondanza, et al.
Human Molecular Genetics|November 3, 2018
The deubiquitinating enzyme Usp14 controls ciliogenesis and Hedgehog signalingFilomena Massa, Roberta Tammaro, Miguel A Prado, et al.
Tissue & Cell|June 1, 2020
The centrosomal/basal body protein OFD1 is required for microtubule organization and cell cycle progressionMariaevelina Alfieri, Daniela Iaconis, Roberta Tammaro, et al.
Developmental Biology|October 6, 2010
Ofd1 is required in limb bud patterning and endochondral bone developmentSabrina Bimonte, Amalia De Angelis, Luca Quagliata, et al.
American Journal of Human Genetics|November 6, 2012
Mutations in COX7B cause microphthalmia with linear skin lesions, an unconventional mitochondrial diseaseAlessia Indrieri, Vanessa Alexandra van Rahden, Valeria Tiranti, et al.
European Journal of Human Genetics : EJHG|April 21, 2026
Revisiting LSDMCA: male lethality escape and genotype-phenotype correlationsAlfonso Manuel D'Alessio, Alessia Indrieri, Giuseppina Vitiello, et al.
Pageof 2